A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359246



Internal ID21016799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99940606..100185299hg38UCSC Ensembl
chr3:99659450..99904143hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38244694
hg19244694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105068
Samples
Known GenesCMSS1, FILIP1L, MIR3921, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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